A Deep Learning Model for Three-Dimensional Determination of Whole Thoracic Vertebral Bone Mineral Density from Noncontrast Chest CT: The Multi-Ethnic Study of Atherosclerosis
- PMID: 40067103
- PMCID: PMC11950887
- DOI: 10.1148/radiol.242133
A Deep Learning Model for Three-Dimensional Determination of Whole Thoracic Vertebral Bone Mineral Density from Noncontrast Chest CT: The Multi-Ethnic Study of Atherosclerosis
Abstract
Background Recent studies have investigated how deep learning (DL) algorithms applied to CT using two-dimensional (2D) segmentation (sagittal or axial planes) can calculate bone mineral density (BMD) and predict osteoporosis-related outcomes. Purpose To determine whether TotalSegmentator, an nnU-net algorithm, can measure three-dimensional (3D) vertebral body BMD across consistently imaged thoracic levels (T1-T10) at any conventional, noncontrast chest CT examination. Materials and Methods This study is a secondary analysis of a multicenter (n = 6) prospective cohort, the Multi-Ethnic Study of Atherosclerosis (MESA). Participants underwent noncontrast chest CT with (n = 296) and without (n = 2660) a phantom. In 594 participants, manual segmentation for T1-T10 vertebrae was performed on axial and sagittal planes. TotalSegmentator provided 3D vertebral body segmentation of T1-T10 levels with further postprocessing to remove cortical bone. Two-dimensional axial and sagittal DL-derived algorithms were developed and compared with 3D model performance. Dice and intersection-over-union scores were calculated. Vertebral BMD-derived data, integrated with the Fracture Risk Assessment Tool with no BMD (FRAXnb), were used to predict incident vertebral fractures (VFx) in participants from the follow-up MESA Examination 6 (n = 1304). Results This study included 2956 participants (1546 [52%] female; age, 69 years ± 9 [SD]), with longitudinal data obtained approximately 6.2 years later in a subset of 1304 participants. DL-derived 3D segmentations were correlated with manual axial (Dice score, 0.93; 95% CI: 0.92, 0.95) and sagittal (Dice score, 0.91; 95% CI: 0.88, 0.93) segmentations. DL-derived 2D axial and sagittal BMD measurements had higher uncertainty compared with DL-derived 3D BMD measurements (average SDs, 2D axial and 2D sagittal vs 3D BMD: 65 mg/cm3 and 59 mg/cm3 vs 41 mg/cm3, respectively; both P < .001). Three-dimensional vertebral BMD with FRAXnb demonstrated better performance in predicting incident VFx (area under the receiver operating characteristic curve [AUC], 0.82) compared with FRAXnb alone (AUC, 0.66; P = .03). Conclusion A multilevel DL algorithm for measuring 3D whole thoracic vertebral BMD using conventional chest CT determined distinct BMD patterns from whole thoracic vertebrae and provided incremental value in predicting VFx. ClinicalTrials.gov identifier: NCT00005487 © RSNA, 2025 Supplemental material is available for this article. See also the editorial by Steiger in this issue.
Conflict of interest statement
References
-
- Sarafrazi N , Wambogo EA , Shepherd JA . Osteoporosis or Low Bone Mass in Older Adults: United States, 2017-2018 . NCHS Data Brief 2021. ( 405 ): 1 – 8 . - PubMed
-
- Gates M , Pillay J , Nuspl M , Wingert A , Vandermeer B , Hartling L . Screening for the primary prevention of fragility fractures among adults aged 40 years and older in primary care: systematic reviews of the effects and acceptability of screening and treatment, and the accuracy of risk prediction tools . Syst Rev 2023. ; 12 ( 1 ): 51 . - PMC - PubMed
Publication types
MeSH terms
Associated data
Grants and funding
- N01 HC095168/HL/NHLBI NIH HHS/United States
- 75N92020D00001/HL/NHLBI NIH HHS/United States
- N01 HC095167/HL/NHLBI NIH HHS/United States
- HHSN268201500003I/HL/NHLBI NIH HHS/United States
- UL1 TR000040/TR/NCATS NIH HHS/United States
- N01 HC095166/HL/NHLBI NIH HHS/United States
- N01 HC095160/HL/NHLBI NIH HHS/United States
- 75N92020D00002/HL/NHLBI NIH HHS/United States
- HHSN268201500003C/HL/NHLBI NIH HHS/United States
- N01 HC095161/HL/NHLBI NIH HHS/United States
- 75N92020D00005/HL/NHLBI NIH HHS/United States
- UL1 TR001079/TR/NCATS NIH HHS/United States
- N01 HC095169/HL/NHLBI NIH HHS/United States
- N01 HC095159/HL/NHLBI NIH HHS/United States
- 75N92020D00003/HL/NHLBI NIH HHS/United States
- R42 AR070713/AR/NIAMS NIH HHS/United States
- R01 HL146666/HL/NHLBI NIH HHS/United States
- UL1 TR001420/TR/NCATS NIH HHS/United States
- 75N92020D00004/HL/NHLBI NIH HHS/United States
- N01 HC095163/HL/NHLBI NIH HHS/United States
- 75N92020D00007/HL/NHLBI NIH HHS/United States
- N01 HC095162/HL/NHLBI NIH HHS/United States
- 75N92020D00006/HL/NHLBI NIH HHS/United States
- N01 HC095165/HL/NHLBI NIH HHS/United States
- N01 HC095164/HL/NHLBI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
Research Materials